MHC class II proteins mediate cross-species entry of bat influenza viruses

Nature. 2019 Mar;567(7746):109-112. doi: 10.1038/s41586-019-0955-3. Epub 2019 Feb 20.

Abstract

Zoonotic influenza A viruses of avian origin can cause severe disease in individuals, or even global pandemics, and thus pose a threat to human populations. Waterfowl and shorebirds are believed to be the reservoir for all influenza A viruses, but this has recently been challenged by the identification of novel influenza A viruses in bats1,2. The major bat influenza A virus envelope glycoprotein, haemagglutinin, does not bind the canonical influenza A virus receptor, sialic acid or any other glycan1,3,4, despite its high sequence and structural homology with conventional haemagglutinins. This functionally uncharacterized plasticity of the bat influenza A virus haemagglutinin means the tropism and zoonotic potential of these viruses has not been fully determined. Here we show, using transcriptomic profiling of susceptible versus non-susceptible cells in combination with genome-wide CRISPR-Cas9 screening, that the major histocompatibility complex class II (MHC-II) human leukocyte antigen DR isotype (HLA-DR) is an essential entry determinant for bat influenza A viruses. Genetic ablation of the HLA-DR α-chain rendered cells resistant to infection by bat influenza A virus, whereas ectopic expression of the HLA-DR complex in non-susceptible cells conferred susceptibility. Expression of MHC-II from different bat species, pigs, mice or chickens also conferred susceptibility to infection. Notably, the infection of mice with bat influenza A virus resulted in robust virus replication in the upper respiratory tract, whereas mice deficient for MHC-II were resistant. Collectively, our data identify MHC-II as a crucial entry mediator for bat influenza A viruses in multiple species, which permits a broad vertebrate tropism.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CRISPR-Associated Protein 9
  • CRISPR-Cas Systems
  • Chickens / genetics
  • Chickens / immunology
  • Chiroptera / genetics
  • Chiroptera / immunology
  • Chiroptera / metabolism
  • Chiroptera / virology*
  • Female
  • Gene Expression Profiling
  • HLA-DR Antigens / genetics
  • HLA-DR Antigens / immunology
  • HLA-DR Antigens / metabolism
  • Histocompatibility Antigens Class II / genetics
  • Histocompatibility Antigens Class II / immunology
  • Histocompatibility Antigens Class II / metabolism*
  • Host Specificity* / genetics
  • Host Specificity* / immunology
  • Humans
  • Influenza A virus / immunology*
  • Influenza A virus / physiology*
  • Male
  • Mice
  • Mice, Knockout
  • Respiratory System / virology
  • Swine / genetics
  • Swine / immunology
  • Viral Tropism / genetics
  • Viral Tropism / immunology
  • Virus Replication
  • Zoonoses / genetics
  • Zoonoses / immunology*
  • Zoonoses / metabolism
  • Zoonoses / virology*

Substances

  • HLA-DR Antigens
  • Histocompatibility Antigens Class II
  • CRISPR-Associated Protein 9